US2919284A

US2919284A - Dibenzacedianthrone

Info

Publication number: US2919284A
Application number: US686832A
Authority: US
Inventors: Caliezi Armin
Original assignee: Ciba AG
Current assignee: BASF Schweiz AG
Priority date: 1956-10-04
Filing date: 1957-09-30
Publication date: 1959-12-29
Anticipated expiration: 1976-12-29

Description

United States Patent DIBENZACEDIANTHRONE Armin Caliezi, Basel, Switzerland, assignor to Ciba Limited, Basel, Switzerland, a firm of Switzerland No Drawing. Application September 30, 1957 Serial No. 686,832

Claims priority, application Switzerland October 4, 1956 1 Claim. (Cl. 260-351) This invention provides new dyestuffs of the acedianthrone series which probably correspond to the general formula (6) v 7 V R V I I 7 0:200]: v CH3 7 I "ice I The compounds of Formula 2 used as starting materials 7 for the present process can be obtained by condensation of the anthrones of the formula or carboxylic acids of the formula with glyoxal or an agent providing glyoxal, for example glyoxal sulfate. obtained eitherby reduction of the corresponding anthrav quinone with nascent hydrogen or by treatment of a compound of the Formula 5 with an agent splitting off water,

for example sulfuric acid or hydrofluoric acid.

The compound of the Formula} can be obtainedby treatment 'of the compound of the Formula 2 with alkaline condensing agents, for example with an alkali metal hydroxide. I

In the above formula a heterocyclic ring system, for example an oxazole,

oxine ring. 7

The ring closure of the compounds of the Formulae 2 and 3 to the acedianthrones can be carried out by ens-t tomary methods by heating with acid condensing agents, such as aluminum chloride, sulfuric, acid, chlo'rsulfonic acid, preferably in the presence of an oxidising agent, for" example per-sulfuric acid, sulfur trioxide, or in an orgarlic solvent such as nitrobenzene, tetrachlorethane, in: the presence of an acid anhydride or acid chloridesuch as P 0 or acetic anhydride and/or sulfuric acid.

With the compounds of the Formula 1 obtained the process of the invention if desired further reactions can be carried out. Thus, for example, they can be treated withhalogenating or nitrating agents. With the resulting halogen-containing or nitro group-containing compounds, still further reactions can be carred out, for example the nitro groups can be reducedand the resulting acedianthrones containing amino groups can be acylchlorides or anthraquiated, for example with benzoyl none carboxylic acid chlorides. H

The compounds of the Formula to the invention, and also the products obtained therefrom by further reactions, constitute valuable vat dyestufis which are suitable for the dyeing of a wide variety of materials, especially for the dyeing and printing of fibers of natural and regenerated cellulose and are also suitable as pigments.

Whereas with other derivatives of =acedianthrone red brown dyeings are obtained, the dyeings from the dyestufis obtained according to the present invention are surprisingly distinguished by very desirable black brown shades.

The following examples illustrate the invention, the parts and percentages being by weight unless otherwise stated and the relation between part by weight and part by volume being the same as that between the kilogram and the liter,

The anthrone of the Formula 4 can be' R indicates a ring system con; sisting of 5- or 6-membered rings,vfor example anatomatic system, such as a benzene or naphthalene ring or 1, obtained according Example 1 'Into a solution of- 60 parts of nitrobenzene, '5 parts of 96% sulfuric acid and 13 parts of acetic anhydride are introduced 5 parts of bis-(1:2'-benzanthronylidene- 10)-etha'1ie',obtained by condensation of 2 mols of 1:2- b'enzanthrone-9 withl 'mol of glyoxal ,sulfatein glacial acetic acid. The mixture is heated within 1%. hours to in glacial acetic acid.

Example 2 3.5 parts of the product prepared according to Example 1 are dissolved in 70 parts of 96% sulfuric acid and treated slowly at 5 C. with 0.5 part of 98.7% nitric acid. Stirring is then carried out for'2 hours at 0-5" C. and then for 17 hours at 20 C. and the reaction product is poured into water. The precipitated substance is washed-with water and then heated for l hour to 55. C. ina solution of 300 parts ofwater, 30 part'sof 30% sodium hydroxide-solution and'20 parts ofsodium hydrosulfate. The leuco compound produced is oxidised by addition of the sodium salt of m-nitrobenzene sulfonic acid. The product is then filtered 01f, washed until neutral and-dried. It is a monoamino derivative.

Example 3 2 parts of the product prepared according to'Example' 2 are heated within 1 hour to 100 C. in 30 parts of nitrobenzene in the presence of 0.65 part of 1-nitroanthraquinone-2-carboxylic acid chloride. Then a further 0.65 part of 1-nitroanthraquinone-2-carboxylic acid chloride is introduced and the whole heated within 3 hours to 200205 C. and stirred for 17 hours at this temperature. Cooling is then carried out to 70 C. and the: dyestutf filtered and washed consecutively with nitrobenzene, alcohol, warm 5% ammonia and water. After drying, a black brown powder is obtained which dyes cotton from the vat in dark brown fast shades.

By using as acylating agent in the preceding paragraph benzoyl chloride, p-chlorobenzoylchloride or terephthaloyl chloride brown dyestufis having similar properties are obtained.

. Example 4 1 part of the dy'estuff produced as described in Example 1 is dissolved in parts by volume of chlorosulfonic acid and the solution is treated at 0-5 C. with 0.42 part of bromine and a trace' of iodine. allowed to rise overnight to C. and the whole then heated for an hour at 50 C. After the customary isolatio'n 1.4 parts of a product are obtained which dyes cotton in reddish brown shades.

The temperature is 4 Example 5 1 part of the dyestuflf obtained according to Example-1 is vatted in 100 parts of water at 45 C. with 2 parts of sodium hydrosulfite with the addition of 4 parts by volume of 30% sodium hydroxide solution. The resulting stock vat is added to a solution of 4 parts by volume of 30% sodium hydroxide solution and 2 parts of sodium hydrosulfite in 2,000.parts of water. In the resulting dye bath 100 parts of cotton aredyed for 1 hourhat-40a-50," Clwith. the addition of. 10 parts of sodium chloride. The cotton is then squeezed ofi, oxidised in the air, rinsed, acidifiedfrinsed' again and soaped atthe boil. It is dyed in violet brown shades of outstanding fastness properties.

Example 6 200 parts of the finely divided dyestulf obtained according to Example 1 are mixed to a paste with 100 parts of Water, 600 parts of a potash thickening (prepared from l-parts of'wheat starch, 330 parts ofwater, parts of glycerol, parts of British gum, parts of tragacanth mucilage and 170 parts of potassium carbonate) and 100 parts of hydrosulfite. A cotton fabric is printed with this paste. After printing, drying is carried out at moderate heat and then steaming at l01l03 C. for 5-10 minutes in air-free Wet steam, rinsing in running water and soaping at the boil. A strong, fast violet brown print is obtained.

What is claimed is:

The vat dyestufi of the formula Zerweck et al.: German Patent App. C 5764 IV 6/22b, Oct. 13, 1955.

672,905 May 28, 1952